Literature DB >> 6790551

Congenital pseudarthrosis of the tibia.

R T Morrissy, E J Riseborough, J E Hall.   

Abstract

Forty cases of congenital pseudarthrosis of the tibia were reviewed. The results were assessed so as to emphasise function rather than simply the presence or absence of union. At the time of review, 14 patients had undergone amputation; eight others had non-union or tenuous union. No surgical procedure except the Farmer operation (a composite skin and bone pedicle graft from the other leg) showed any clear superiority. Among the factors associated with a poor result were considerable shortening, older children, and rapid resorption of the bone graft. It is felt that congenital pseudarthrosis of the tibia is a biological problem and not merely a mechanical one; consequently biological approaches to its treatment are needed.

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Year:  1981        PMID: 6790551     DOI: 10.1302/0301-620X.63B3.6790551

Source DB:  PubMed          Journal:  J Bone Joint Surg Br        ISSN: 0301-620X


  15 in total

1.  Pediatric 25-hydroxyvitamin D concentrations in neurofibromatosis type 1.

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Journal:  J Pediatr Endocrinol Metab       Date:  2011       Impact factor: 1.634

2.  Pediatric microsurgery.

Authors:  J A Diez Pardo
Journal:  World J Surg       Date:  1985-04       Impact factor: 3.352

Review 3.  Ilizarov treatment of congenital pseudarthrosis of the tibia: a multi-targeted approach using the Ilizarov technique.

Authors:  In Ho Choi; Tae-Joon Cho; Hyuk Ju Moon
Journal:  Clin Orthop Surg       Date:  2011-02-15

4.  A short series of congenital pseudoarthrosis tibia.

Authors:  Jagdish Patwa; Reeny Patel
Journal:  J Orthop       Date:  2013-09-14

Review 5.  A genetic study of von Recklinghausen neurofibromatosis in south east Wales. II. Guidelines for genetic counselling.

Authors:  S M Huson; D A Compston; P S Harper
Journal:  J Med Genet       Date:  1989-11       Impact factor: 6.318

6.  Congenital pseudarthrosis of the tibia: the results of an evolving protocol of management.

Authors:  N Nicolaou; A Ghassemi; R A Hill
Journal:  J Child Orthop       Date:  2013-06-12       Impact factor: 1.548

7.  Hyperactive transforming growth factor-β1 signaling potentiates skeletal defects in a neurofibromatosis type 1 mouse model.

Authors:  Steven D Rhodes; Xiaohua Wu; Yongzheng He; Shi Chen; Hao Yang; Karl W Staser; Jiapeng Wang; Ping Zhang; Chang Jiang; Hiroki Yokota; Ruizhi Dong; Xianghong Peng; Xianlin Yang; Sreemala Murthy; Mohamad Azhar; Khalid S Mohammad; Mingjiang Xu; Theresa A Guise; Feng-Chun Yang
Journal:  J Bone Miner Res       Date:  2013-12       Impact factor: 6.741

8.  Hyperactive Ras/MAPK signaling is critical for tibial nonunion fracture in neurofibromin-deficient mice.

Authors:  Richa Sharma; Xiaohua Wu; Steven D Rhodes; Shi Chen; Yongzheng He; Jin Yuan; Jiliang Li; Xianlin Yang; Xiaohong Li; Li Jiang; Edward T Kim; David A Stevenson; David Viskochil; Mingjiang Xu; Feng-Chun Yang
Journal:  Hum Mol Genet       Date:  2013-07-17       Impact factor: 6.150

Review 9.  The use of anterolateral bowing of the lower leg in the diagnostic criteria for neurofibromatosis type 1.

Authors:  David A Stevenson; David H Viskochil; Elizabeth K Schorry; Alvin H Crawford; Jacques D'Astous; Kathleen A Murray; J M Friedman; Linlea Armstrong; John C Carey
Journal:  Genet Med       Date:  2007-07       Impact factor: 8.822

10.  Evidence of increased bone resorption in neurofibromatosis type 1 using urinary pyridinium crosslink analysis.

Authors:  David A Stevenson; Elisabeth L Schwarz; David H Viskochil; Laurie J Moyer-Mileur; Mary Murray; Sean D Firth; Jacques L D'Astous; John C Carey; Marzia Pasquali
Journal:  Pediatr Res       Date:  2008-06       Impact factor: 3.756

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